Home > Journals > Chirurgia > Past Issues > Chirurgia 2008 June;21(3) > Chirurgia 2008 June;21(3):185-7

CURRENT ISSUE
 

ARTICLE TOOLS

Reprints

CHIRURGIA

A Journal on Surgery


Indexed/Abstracted in: EMBASE, Scopus, Emerging Sources Citation Index

 

CASE REPORTS  


Chirurgia 2008 June;21(3):185-7

Copyright © 2008 EDIZIONI MINERVA MEDICA

language: English

Surgical treatment of middle aortic syndrome: a rare cause of hypertension in childrens

Khan M. Z., Shahabuddin S., Hamid M., Amanullah M. M.

Division of Congenital Cardiac Surgery Department of Cardiac Surgery The Aga Khan University Hospital, Pakistan


PDF  


Middle aortic syndrome is a rare condition characterized by segmental narrowing of descending thoracic aorta or abdominal aorta. It is either congenital or produced by a number of acquired etiologies. The condition may cause severe hypertension and most of the patients if left untreated would die by 40 years of age. A 12 year old girl presented with severe hypertension secondary to discrete mid – thoracic aortic coarctation. We present the surgical technique employed and discuss other modalities of treatment.

top of page

Publication History

Cite this article as

Corresponding author e-mail